Argon Medical Devices recalls 26G PICC catheters labeled 30cm but containing 50cm length, potentially causing procedural delays. Affected units have specific lot and expiration dates.
Peripherally Inserted Central Catheter (PICC) is labeled 26G/1.9Fr x 30cm but package contains incorrect 26G/1.9Fr x 50cm PICC, which could lead to procedural delay.
Argon Medical Devices is recalling a specific type of PICC catheter that was labeled as 30cm but actually contains a 50cm length. This incorrect length could cause delays during medical procedures.
The catheter is labeled as 26G/1.9Fr x 30cm but the actual product contains a 50cm length. This discrepancy could lead to procedural delays during medical procedures.
Healthcare professionals who use this specific PICC catheter model are likely affected. Patients receiving procedures with this catheter may be at risk of procedural delays.
Check for the product name 'L-CATH PICC S/L Peripherally Inserted Central Catheter, 26Ga (1.9F) 0.60mm x 30cm' with reference number 384539. The lot number is 11563923 and expiration date is March 11, 2027.
Verify the product's lot number (11563923) and expiration date (March 11, 2027) against the provided information.
The catheter is labeled as 26G/1.9Fr x 30cm but contains a 50cm length, which could lead to procedural delays.
The recall record does not specify a remedy, so no action is required beyond checking the product details.
The recall states this could lead to procedural delays, but no injury risk is mentioned.
We’ve drafted a message you can send Argon Medical Devices to request your refund or repair — edit it as you like.
Subject: Recall Z-2638-2024 — Argon Medical Devices Argon Medical Devices Hello, I own a Argon Medical Devices that is covered by recall Z-2638-2024 from Argon Medical Devices. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
